State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; University of Chinese Academy of Sciences, Beijing 100049, China.
School of Environment, Guangzhou Key Laboratory of Environmental Exposure and Health, and Guangdong Key Laboratory of Environmental Pollution and Health, Jinan University, Guangzhou 510632, China.
Environ Pollut. 2016 Nov;218:1108-1115. doi: 10.1016/j.envpol.2016.08.064. Epub 2016 Sep 2.
Mass transfer of hydrophobic organic contaminants (HOCs) across the air-water interface is an important geochemical process controlling the fate and transport of HOCs at the regional and global scales. However, few studies have characterized concentration or fugacity profiles of HOCs near both sides of the air-water interface, which is the driving force for the inter-compartmental mass transfer of HOCs. Herein, we introduce a novel passive sampling device which is capable of measuring concentration (and therefore fugacity) gradients of HOCs across the air-water interface. Laboratory studies indicated that the escaping fugacity values of polycyclic aromatic hydrocarbons (PAHs) from water to air were negatively correlated to their volatilization half-lives. Results for field deployment were consistent between the passive sampler and an active method, i.e., a combination of grab sampling and liquid-liquid extraction. In general, the fugacity profiles of detected PAHs were indicative of an accumulation mechanism in the surface microlayer of the study regions (Haizhu Lake and Hailing Bay of Guangdong Province, China), while p,p'-DDD tended to volatilize from water to the atmosphere in Hailing Bay. Furthermore, the fugacity profiles of the target analytes increased towards the air-water interface, reflecting the complexity of environmental behavior of the target analytes near the air-water interface. Overall, the passive sampling device provides a novel means to better characterize the air-water diffusive transfer of HOCs, facilitating the understanding of the global cycling of HOCs.
疏水性有机污染物(HOCs)在气-水界面的传质是控制 HOCs 在区域和全球尺度上归宿和迁移的一个重要地球化学过程。然而,很少有研究描述 HOCs 在气-水界面两侧的浓度或逸度分布,而这正是 HOCs 在隔室间进行质量传递的驱动力。在此,我们引入了一种新的被动采样装置,该装置能够测量 HOCs 在气-水界面的浓度(因此也是逸度)梯度。实验室研究表明,多环芳烃(PAHs)从水中逸入空气中的逸度值与其挥发半衰期呈负相关。现场部署的结果与主动方法(即采集和液-液萃取的组合)一致。总的来说,所检测到的 PAHs 的逸度分布表明在研究区域(中国广东的海珠湖和海陵湾)的表面微层中存在一种积累机制,而 p,p'-DDD 则倾向于从水中挥发到大气中。此外,目标分析物的逸度分布朝着气-水界面增加,反映了目标分析物在气-水界面附近环境行为的复杂性。总的来说,被动采样装置为更好地描述 HOCs 的气-水扩散迁移提供了一种新方法,有助于理解 HOCs 的全球循环。